Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism

Complex chromosomal rearrangements involve the restructuring of genetic material within a single chromosome or across multiple chromosomes. These events can cause serious human disease by disrupting coding DNA and gene regulatory elements via deletions, duplications, and structural rearrangements. Here we describe a 5-year-old female with severe developmental delay, dysmorphic features, multi-suture craniosynostosis, and growth failure found to have a complex series of balanced intra- and inter-chromosomal rearrangements involving chromosomes 4, 11, 13, and X. Initial clinical studies were performed by karyotype, chromosomal microarray, and FISH with research-based short-read genome sequencing coupled with sanger sequencing to precisely map her breakpoints to the base pair resolution to understand the molecular basis of her phenotype. Genome analysis revealed two pathogenic deletions at 4p16.1-p15.32 and 4q31.1, accounting for her developmental delay and dysmorphism. We identified over 60 breakpoints, many with blunt ends and limited homology, supporting a role for non-homologous end joining in restructuring and resolution of the seminal chromoplexy event. We propose that the complexity of our patient’s genomic rearrangements with a high number of breakpoints causes dysregulation of gene expression by three-dimensional chromatin interactions or topologically associating domains leading to growth failure and craniosynostosis. Our work supports an important role for genome sequencing in understanding the molecular basis of complex chromosomal rearrangements in human disease. Supplementary Information The online version contains supplementary material available at 10.1186/s13039-022-00610-4.


Introduction
Microdeletions can produce distinct patterns of malformations and symptomatology secondary to haploinsufficiency of one or multiple genes. Interstitial deletion of 4p14 to 4p16.1 causes a recognizable syndrome of mild to severe intellectual disability, hypotonia, and dysmorphic features, including a long face, upslanting palpebral fissures, a large beaked nose, and a thick lower lip with normocephaly and tall, thin body habitus [6,19,21]. The 4p14p16.1 deletion syndrome is genetically and phenotypically distinct from the neighboring microdeletion syndrome Wolf-Hirschhorn syndrome (WHS) characterized by dysmorphic features termed the "Greek warrior helmet" appearance, growth failure and severe developmental delay caused by heterozygous deletion of 4p16.3 [1]. In contrast to WHS in which clear  Microdeletions involving dominant disease associated genes can arise de novo or can be inherited from a similarly or more mildly affected parent. Microdeletions occur as an isolated event, derive from an unbalanced chromosome translocation, or arise in association with complex chromosomal rearrangements [24]. While most balanced rearrangements are not associated with a clinical phenotype, the presence of cryptic copy number variation at the breakpoints is seen in approximately 40% of individuals with an abnormal phenotype due to disruption of additional genes and regulatory elements.
Complex chromosomal rearrangements (CCRs) involve a minimum of five breakpoints and in the case of translocations, a minimum of 2 chromosomes. There are many types of CCRs including chromothripsis, chromoplexy, and chromoanasynthesis [24]. Chromothripsis is caused by localized shattering and random reassembly of tens to hundreds of chromosome segments with nonhomologous end-joining or microhomology-mediated end-joining, and can lead to multiple deletions [10,17]. Chromoplexy, involving multiple chromosomes and primarily reported in somatic cells, is believed to arise secondary to aberrant transcription factor binding leading to the formation of two or more chimeric chromosomes [2]. Chromoanasynthesis is thought to be caused by polymerase stalling leading to localized duplications and triplications often accompanied by chromosome translocations [15]. CCRs are believed to arise from the imperfect repair of a single, catastrophic genomic event [2,15,17]. These events play critical roles in genome evolution, as well as human disease, including cancer. Of the three classes of CCRs, chromothripsis is most frequently reported in literature.
Here we present a 5-year-old female with severe global developmental delay, growth failure, craniosynostosis and dysmorphic features found by karyotype, microarray and FISH testing to have de novo deletions at 4p16.1-p15.32 (9.76 Mb), 4q31.1 (881 Kb), and 11q22.1 (771 Kb) that likely occurred as part of a complex chromoplexy event involving four chromosomes. Her clinical presentation of severe growth failure and craniosynostosis could not be explained by her microdeletions. We performed research-based short-read paired-end genome sequencing and Sanger sequencing to better characterize her breakpoints and deletions. We identified 62 break sites, suggesting previously unappreciated complexity to her genomic rearrangement. We propose that more advanced sequencing methodologies are an important tool for understanding the phenotypes of complex chromosomal rearrangements.

Chromosome microarray analysis (CMA)
An Illumina Infinium Global Screening Array (GSA; Illumina, San Diego, Calif ) was used to obtain research chromosomal microarray analysis (CMA) for the proband and unaffected parents. The PennCNV algorithm [20] was used for CNV calling. Briefly, log R ratios were used to determine the dosage by intensity of signal, and B allele frequency was calculated using genotype clusters per SNP as determined from HapMap sample analysis. Clinical CMA was independently performed using the Illumina 850 k v1.1 array. Resulted CNVs were interpreted for their pathogenicity by using publicly available databases (DECIPHER, ClinVar, and DGV).

Short-read genome sequencing and structural variations (SVs) analysis
Whole genome sequencing was performed using the Twist Library Preparation Kit (TWIST Bioscience) and Illumina NovaSeq 6000 at the Center for Applied Genomics (CAG) at the Children's Hospital of Philadelphia (CHOP). Data were quality controlled and analyzed using a custom-built pipeline [13] that incorporates BWA-mem v0.7.12 [14] for alignment and Picard v1.97 for PCR duplication removal. BAM files generated were fed to short-read structural variant callers, including Manta [3] and Wham [11], to capture SVs with default parameters. Similarly, the split and discordant read files were generated by SpeedSeq [5] and provided as inputs to Lumpy [12], another SV calling program.

Sanger sequencing of breakpoints
Breakpoint PCR primers were designed using primer 3 and amplicons were sequenced with forward and reverse primers following standard protocols. The UCSC BLAT tool was used to analyze the breakpoints.

Patient presentation
The proband was naturally conceived to a 28-yearold G3P1-> 2 mother. There was a history of one prior miscarriage at 8 weeks gestation. Pregnancy was complicated by maternal Rh-negative status treated with Rhogam and ventriculomegaly detected on 20-week ultrasound. Follow up fetal MRI and echocardiogram were normal. Intrauterine growth restriction was noted during the third trimester. Noninvasive prenatal testing (NIPT) for Trisomy 13, 18, 21 and sex-chromosome aneuploidy done at 20 + 1 week gestation was normal.
The proband was born via Caesarian section at 36 2/7 weeks gestational age for breech presentation and persistent intrauterine growth restriction. Birth weight was 1295 g (< 1%; Z = − 2.73), length was 38 cm (< 1%; Z = − 3.63), and head circumference was 29.5 cm (4%; Z = − 1.78). APGAR scores were 8 and 9 at one and 5 min of life, respectively. Physical examination was notable for splayed sagittal sutures, a flattened occiput, large posterior fontanel, down-slanting palpebral fissures, lowset and posteriorly rotated ears, a triangular chin, bilateral 2,3 toe syndactyly and mild head lag. The proband developed conjugated hyperbilirubinemia and was noted to have splenomegaly, prompting abdominal ultrasound, which showed a normal liver and enlarged spleen. A metabolic workup was initiated and was non-diagnostic. Chromosomal SNP microarray was ordered and showed three novel interstitial copy number variations involving chromosomes 4 and 11. Follow up G-banding and FISH analysis showed a complex karyotype involving multiple rearrangements between chromosomes 4, 11, 13 and X consistent with a catastrophic genome wide event to be discussed in greater detail below.
The proband was re-evaluated by Clinical Genetics at 27 months of age. Growth parameters were notable for a weight of 6.485 kg (< 1%; Z = − 7.78), a length of 72 cm (< 1%; Z = − 4.31), and a head circumference of 40.5 cm (< 1%; Z = − 4.76). Physical examination was notable for brachycephaly, prominent sagittal sutures, proptosis with inability to fix or follow, blue sclera, thin skin with prominent veins, sparse hair, and severe hypotonia. Clinical course had evolved to include obstructive sleep apnea with nocturnal CPAP dependence improved by tonsillectomy and adenoidectomy, optic atrophy with preserved visual responsiveness, conductive hearing loss status post bilateral myringotomy tube placement, tethered cord status post release, anemia, thrombocytopenia, hepatosplenomegaly, milk protein intolerance, severe failure to thrive with G-tube dependence, severe global developmental delay, and self-injurious behavior. Additionally, she had Kawasaki disease complicated by dilation of the aortic root, ascending aorta, and coronary arteries. Due to proptosis and prominent sagittal sutures, she was evaluated by Plastic Surgery, and was found to have multisuture craniosynostosis involving the sagittal and coronal sutures.
At 5 years of age, the proband presented with a weight of 12.6 kg (1%; Z = − 3.08), a length of 89.5 cm (< 1%; Z = − 4.08), and a head circumference of 47 cm (< 1%; Z = − 2.39). Physical examination was unchanged, with mild proptosis, down-slanting palpebral fissures, absent fixing and following, hypertelorism, and severe hypotonia (Fig. 1). Her clinical course had evolved to also include chronic constipation with normal barium enema, recurrent C. difficile infection, chronic, patchy inflammatory changes with duodenitis on colonoscopy and esophagogastroduodenoscopy, TPN dependence, postprandial hypoglycemia with a normal metabolic evaluation, chronic aspiration, oral aversion, chronic otitis media status post bilateral myringotomy tube placement, mild-moderate conductive hearing loss requiring hearing aids, and abnormal EEG showing diffuse and focal cerebral dysfunction with no seizures.

Research genome sequencing
To map the exact breakpoints of the putative deletions detected by the clinical chromosomal microarray analysis, we performed short-read WGS analysis of the proband and her parents. The average sequencing depth was 28.1x, 26.2x, and 30.2x for proband, mother, and father, respectively. SV calling based on read depth, paired-end read discordance, split-reads, and assembly approaches extended the 9.76 Mb deletion and PCR/ Sanger sequencing precisely determined that the deletion is chr4(GRCh37):g.7,145,092-16,910,359 with blunt ends at the breakpoint (Fig. 3). The two smaller deletions of unknown significance at 4q31.1 and 11q22.1q22.2 were not detected by three algorithms (Lumpy, Manta, and Wham). We then manually reviewed the depth of the whole genome level plotted by using kpPlotBAMDensity in an R package karyoploteR. The 9.76 Mb deletion of 4p16.1p15.32 and the deletion at 4q31.1 were evident on the proband's depth plot (Fig. 4a, upper panel), but not the deletion at 11q22.1q22.2 (data not shown). This prompted us to pursue an independent chromosomal microarray analysis with Illumina Infinium Global Screening Array, which did confirm the two smaller deletions (Fig. 4a, lower panel; and Fig. 4b).

Breakpoint mapping of complex rearrangements at nucleotide resolution
To obtain detailed insights into the complex rearrangements suggested by the karyotype and FISH analyses and to identify possible genetic candidate(s) for the patient's unusual clinical phenotype, we comprehensively analyzed the putative de novo structural variations (SVs) from the trio WGS data. SV calling based on multiple approaches suggested six additional deletions, seven duplications, one inversion, six interchromosomal translocations, and 18 one-sided inversion break ends, all de novo in the proband. Interestingly, the majority of these structural rearrangements (5/6 deletions, 7/7 duplications, 1/1 inversion, 6/6 interchromosomal events, and 12/18 one-sided inversion break ends) involved chromosome 4 and overlapped substantially at 4p15 and 4q31q35. Since short-read WGS analysis successfully identified relatively precise breakpoints, PCR/Sanger sequencing was subsequently performed to further clarify these overlapping events. Remarkably, all putative structural rearrangement events, except two (n = 30), were confirmed at the nucleotide level with patient-specific PCR products (Additional file 1: Figure S3 and Additional file 1: Table S1) in 37 successful PCR/Sanger assays, revealing 56 breakpoints in total. Including the six breakpoints generated by the three aforementioned deletions, the patient has 62 breakpoints, with 68% (42/62) of Many of the putative chromosome 4 SVs overlapped substantially, and this is incompatible with the diploid genome. We then reviewed the genome depth plot and alignment for these so-called putative deletions and duplications by the SV calling algorithms and identified no supportive depth drop or evidence of gain (data not shown), suggesting that the breakpoints were not forming conventional SVs, but rather indicative of intrachromosomal and interchromosomal recombinations.
All of the 58 Sanger confirmed breakpoints had either blunt ends or 1-4 bp microhomology sequences with two small insertions (1 and 52 bp) (Additional file 1: Figure S3). All of these breakpoints tended not to cluster at a certain location of the affected chromosome, and the majority of rearrangements led to minimal copy number changes, suggesting that breakpoints were resolved through non-homologous end-joining, consistent with the known mechanism of chromoplexy.
We identified 16 protein-coding genes disrupted by at least 1 breakpoint, 8 of which are associated with human disease (Additional file 1: Table S2) Among them, only SRP72 and SGMS2 are associated with autosomal dominant inheritance; however, both genes have a pLI score inconsistent with haploinsuffciency, and the associated phenotypes (bone marrow failure syndrome and calvarial doughnut lesions with bone fragility) have no overlap with our proband (Additional file 1: Table S2). Four gene fusions were identified with three of those fused genes being fused in an incompatible orientation, and thereby unlikely to have a stable RNA transcribed, leaving only one candidate with compatible orientation, a ALKBH8-BIRC2 fusion. The function of such a fusion protein is unknown.

Discussion
Here we describe a 5-year-old female with severe developmental delay, growth failure, dysmorphic features, and craniosynostosis found by karyotype, microarray, FISH, and genome sequencing to have three microdeletions and multiple intra-and inter-chromosomal recombinations consistent with a catastrophic chromoplexy event involving at least 4 chromosomes. Careful mapping of her breakpoints demonstrated multiple blunt end breaks with small insertions, suggesting that nonhomologous end joining was the mechanism underlying the genome breaks, consistent with our understanding of chromoplexy. While many of her translocations are of unclear clinical significance, her interstitial deletion of 4p16.1p15.32 is classified as pathogenic.
Deletions involving the short arm of chromosome 4 result in at least two clinically distinct syndromes: WHS caused by heterozygous deletion of a 165 Kb critical region (minimum) within 4p16.3 characterized by dysmorphisms, seizures, growth failure, and global developmental delay, and interstitial 4p deletion syndrome involving a genomic region proximal to the WHS critical region characterized by distinct dysmorphic features and developmental delay with normal growth parameters. Our patient's 4p deletion does not overlap with the WHS critical region, but does include the proximal 4p interstitial deletion critical region, and this likely explains some of her dysmorphic features and developmental delay ( Table 1). Of note, growth failure and craniosynostosis are not features of the proximal 4p deletion syndrome.
To better understand the molecular basis of our patient's phenotype we performed genome sequencing to more accurately define the breakpoints and rearrangements of genes and regulatory regions. A likely candidate was our patient's deletion at 4q31.1, which includes seven genes (MGARP, NDUFC1, NAA15, RAB33B, SETD7, MGST2, and MAML3). Since the initial clinical array was performed, haploinsufficiency of NAA15 has been  [4,18]. We therefore reclassify the patient's 4q31 deletion as pathogenic and suggest that it contributes to our patient's global delays ( Table 2). The patient's deletion [chr11(GRCh37 ):g.101,524,246-102,235,141] at 11q22.1q22.2 includes six protein-coding genes (ANGPTL5, CEP126, CFAP300, YAP1, BIRC3, and BIRC2). YAP1 has been associated with autosomal dominant coloboma with variable penetrance (MIM 120433), and has a pLI score of 1. Associated phenotypes include isolated ocular coloboma with variable penetrance or coloboma with sensorineural hearing loss, cleft lip/palate, and learning difficulties [22]; however, YAP1 gene deletion has been reported in a healthy subject [23], and review of our internal SNP microarray dataset (> 21,000 individuals) revealed two other healthy subjects harboring heterozygous deletions of the YAP1 gene (data not shown). Thus, we consider the deletion at 11q22.1q22.2 a variant of uncertain significance.
Our patient has two large, pathogenic deletions, and it is possible that her severe phenotype relates to a compound effect of both variants. Additive effects of multiple genetic hits have been described for ciliopathy syndromes, hearing loss, and neurodevelopmental disorders; however, in most cases phenotypes are exacerbated by dual hits, but they are not altogether novel, as is the case in our patient. We used short-read genome sequencing and extensive Sanger sequencing to identify critical regulatory regions or novel breakpoints to explain our patient's atypical phenotype and identified greater than 60 breakpoints across 4 chromosomes with multiple gene fusions and complex rearrangements. Though no distinct causal gene was identified, these methodologies established a higher resolution map of our patient's genomic rearrangements and revealed far greater complexity than that ascertained by clinical testing. The complexity of our patient's chromoplexy event and its resolution may ultimately be the explanation for her unique phenotype of growth failure and craniosynostosis. For example, genes associated with these phenotypes may be dysregulated without being disrupted by a breakpoint. Structural rearrangements, including complex chromosomal rearrangements, have been shown to dysregulate gene expression through disruption of three-dimensional chromatin interactions, or topologically associating domains [9,16]. We queried the ENCODE data to assay for three-dimensional CTCF-bound topologically associated domains (TAD) for these 62 breakpoints and identified one breakpoint that occurred in a cis-regulatory element (ccRE; ENCODE accession number EH38E2348238). This ccRE has a maximum CTCF Z score of 4.17, highly suggestive that it has CTCF-bound insulator property. Nearby protein-coding genes include CDKN2AIP, ING2, CLDN24, WWC2, CLDN22, RWDD4, TRAPPC11, STOX2, DCTD, TENM3, ENPP6, and IRF2. Though many of these genes are involved in growth and cell cycle regulation, further evaluation of the possible contribution of this ccRE to the phenotype is needed.
We noted that several genes on chromosomes 4 and 11 have been associated with craniosynostosis, including FGFR3, WDR19, PPP3CA, SEC24D, SOX6, ALX4, and B3GAT3. Analysis of the mRNA gene expression or protein levels of these genes in the relevant patient cells compared to control samples in combination with ccRE analysis may be revealing for her craniosynostosis phenotype.
Our study has several limitations. We did not perform PacBio long-read genome sequencing, optical mapping, or mate-pair short-read genome sequencing, which, if combined with molecular cytogenic techniques, may have provided additional delineation of the structure of the derivative chromosomes or identified additional  [7,8]. Additionally, short-read genome sequencing analysis based on splitread, depth, and assembly methods was unable to identify the small deletions on chromosomes 4 and 11. This was overcome by concurrent use of cytogenetic assays (including FISH and SNP microarray), highlighting the importance of multiple, synergistic approaches when evaluating complex patients and characterizing complex chromosomal aberrations. In summary, we present a case of a complex genomic rearrangement causing severe neurodevelopmental delays and growth failure in a young child. Our results suggest that the use of short-read paired-end genome sequencing can help resolve individual breakpoints and better establish the molecular etiology of patient phenotypes.
Additional file 1 Additonal genomic data.